A5079221946- Enzyme Production and Characterization
- Carbohydrate Chemistry and Synthesis
- Glycosylation and Glycoproteins Research
- Microbial Metabolites in Food Biotechnology
- Enzyme Catalysis and Immobilization
- Analytical Chemistry and Chromatography
- Biofuel production and bioconversion
- Radiation Effects and Dosimetry
- Drug Solubulity and Delivery Systems
- Biopolymer Synthesis and Applications
- Proteoglycans and glycosaminoglycans research
- Advanced Drug Delivery Systems
- Polysaccharides Composition and Applications
- Diet, Metabolism, and Disease
- Food composition and properties
- Polysaccharides and Plant Cell Walls
- Microencapsulation and Drying Processes
- Proteins in Food Systems
- Chemical Synthesis and Analysis
- Surfactants and Colloidal Systems
- biodegradable polymer synthesis and properties
- Lipid Membrane Structure and Behavior
- Amino Acid Enzymes and Metabolism
- Bee Products Chemical Analysis
- Insect and Pesticide Research
University College London
2010-2023
Medway School of Pharmacy
2020-2021
University of East Anglia
2006-2018
Norwich Research Park
2017
Birmingham and Midland Eye Centre
1965-2015
Swedish Institute
2009
Chalmers University of Technology
2009
University of Greenwich
2008-2009
University of Birmingham
1979-2005
University of Alberta
2005
S. A. Barker, E. J. Bourne, M. Stacey and D. H. Whiffen, Chem. Soc., 1954, 171 DOI: 10.1039/JR9540000171
This chapter contains sections titled: Introduction Identification and Determination of Carbohydrates Detection Common Substituent Groups Hydrogen Bonding in Cellulose Degree Crystallinity Infrared Analysis Pyranose Derivatives Furanose Conclusions
S. A. Barker, B. Foster, M. Stacey and J. Webber, Chem. Soc., 1958, 2218 DOI: 10.1039/JR9580002218
S. A. Barker, E. J. Bourne, R. Stephens and D. H. Whiffen, Chem. Soc., 1954, 3468 DOI: 10.1039/JR9540003468
Solid dispersion technology represents a successful approach to addressing the bioavailability issues caused by low aqueous solubility of many Biopharmaceutics Classification System (BCS) Class II drugs. In this study, use high-yield manufacture fiber-based is explored as an alternative monolith production methods. A temperature-controlled solvent-free centrifugal spinning process was used produce sucrose-based microfibers containing poorly water-soluble drugs olanzapine and piroxicam (both...
Research Article| May 01 1958 Some paper-chromatographic studies with Aspergillus niger ‘152’ transfructosylase S. A. Barker; Barker 1Chemistry Department, The University, Edgbaston, Birmingham 15 Search for other works by this author on: This Site PubMed Google Scholar E. J. Bourne; Bourne M. Stacey; Stacey R. B. Ward Biochem J (1958) 69 (1): 60–62. https://doi.org/10.1042/bj0690060 Views Icon Article contents Figures & tables Video Audio Supplementary Data Peer Review Share Facebook...
S. A. Barker, E. J. Bourne and M. Stacey, Chem. Soc., 1953, 3084 DOI: 10.1039/JR9530003084
S. A. Barker and E. J. Bourne, Q. Rev. Chem. Soc., 1953, 7, 56 DOI: 10.1039/QR9530700056
There has been increasing interest over recent years in the application of three-dimensional (3D) printing technologies biomedical field. One such method is Direct Ink Writing (DIW); this approach potential advantage allowing room-temperature deposition materials, presented as an ink, to build complex architectures. DIW offers ability process biomaterials containing temperature-sensitive components. Due fabrication principles DIW, there are specific rheological requirements that ink must...
Zein, the main seed storage protein of maize, has been widely studied as a possible source material for production biodegradable plastic films. Plasticization zein is critical to make functional While there have number publications which report behavior systems with wide variety plasticizers, few attempt examine interactions and plasticizer at molecular level. In this paper, we on plasticizing effects water, glycerol, 2-mercaptoethanol, were examined by combination spectroscopy (FTIR...
A liposome system was evaluated for oral delivery of a poorly bioavailable hydrophilic drug. The prepared from proliposome, which consisted negatively charged phosphatidylcholine, whereas cefotaxime chosen as the model An in vivo study carried out on nine rats according to three-way crossover design compare bioavailability liposomal formulation with that an aqueous drug solution and physical mixture blank liposomes. results indicated extent increased approximately 2.7 2.3 times compared...
S. A. Barker and R. Stephens, J. Chem. Soc., 1954, 4550 DOI: 10.1039/JR9540004550